Polymer products



July 23, w46. v l.. HANsLEY POLYMER PRODUCTS Filed Nov. 4, v1944 IN VEN TOR.

'2,404,716 roam/ma raonuc'rs f virgin r.. Hensley, Niagara raus, N. Y., assigner to iE. l. du Pont de Nemours & Company, Wilmington, Del.,a corporation of Delaware Application November 4, 1944, Serial No. 562,01:

V15.7 Claims.

This invention relates to a new composition of gisant (Cl. 26o- 32) matter and shaped articles produced therefrom.'

Polyacrylonitrile, and copolymers and inter-- l polymers of acrylonitrile with other polymerizable substances, for example vinyl or` acrylic compounds in which at least 85% by weight of the polymer is acrylonitrile have been known for some time and recognized as possessing desirable physical and chemical properties including toughness and insolubility in and insensitivity to common organic solvents such as methyl or ethyl alcohol, acetone, ethyl ether, ethyl acetate, hydrocarbon solvents, chlorinated hydrocarbons Iand the like. Because of these facts, numerous attempts have been made to form these polymeric materials into yarns, films and other Vshaped articles. f

The copending application of George H.

Latham, Serial No. 562,012, filed of even date herewith discloses solutions of polyacrylonitrile in dimethyl carbamyl compounds and the production of extruded and otherwise shaped articles and structures from such solutions. The abovesaid application of George H. Latham represents the rst successful dissolution of polyacrylo'- nitrile in a solvent to produce a solution which is suitable for the production'of commercially useful textile yarns 0r wrapping tissue films, and

similar tough, exible structures.

The present application relates to a similarly satisfactory dissolution of polyacrylonitrile in an organic solvent taken from a different class of organic compounds and the polyacrylonitrile solutions produced thereby are similarly satisfactory for the production of tough, flexible, dense, colorless yarns andiilms which are suitable for vuse in practically all general commercial applications of such products. v

It has been known heretofore that concentrated aqueous solutions of inorganic saltssuch as lithium bromide, zinc chloride and sodium sulfocyanide will dissolve polyacrylonitrile and it has been proposed (Rein U. 5. Patent No. 2,140,921) to employ the resulting solutions in the formation of yarns and lms. However, it has been found substantially impossible to use the resulting compositions in such-a manner. Their extrusion into coagulating baths of the type proposed V(including such non-solvents for acrylonitrile as water, dilute acid, dilute salt solutions, etc.) result in the formation of shaped articles that contain large amounts of the inorganic salt of the proposed solvent. These saltsare distributed throughout the structure and destroy the continuity ofthe polyarcylonitrile phase and the structure possesses poor physical properties. Removal of these salts, when possible, results in the formation of a porous, spongy, Weak, undesirable structure that is very brittle and completely unsuited for use as a yarn or film. Moreover, when it is attempted to form a multiilament yarn byv extruding, for example the proposed aqueous sodium sulfocyanide polyacrylonitrile composition', into a dilute acid bath, it is found that the individual filaments obtained stick together to form an essentially monofllament structure that is extremely brittle and cannot be bent or worked without breaking.

U. S. Patent No. 2,167,537 to Tobls points out that certain copolymers of acrylonitrile and an acrylic acid ester (those copolymers containing l not more than 65% of acrylonitrile) are soluble in' mixtures of organic solvents such 'as dioxan,

monochlorbenzene, cyclohexanone, etc, `How Y ever, these liquids are incapable of dissolving or even swelling polyacrylonitrile or copolymers of acrylonitrile 'containing higher percentages of acrylonitrile, i. e. acrylonitrile polymers of the type with which this invention is concerned. As previously mentioned, polymers containing such high percentages (at least 85% by weight) of acrylonitrile are especially desirable for use because of their good physical properties and excellent chemical resistance.

It has also been proposed (Rein U. S. Patent No. 2,117,210) to dissolve polyacrylonitrile in molten quatemary ammonium salts such as benzyl pyridinium chloride, an ionizable salt. Al-

though the resulting solution can allegedly be used to form yarns or films of polyacrylonitrile,

and very weak, presumably because of the presence within them of residual quaternary ammonium salt. Removal of this salt is difllcult and the resulting structures contain numerous and large voids that make the structures substantially useless for commercial purposes.

It is therefore an object of this invention to dissolvel polyacrylonitrile ora copolymer or interpolymer of acrylonitrile in which at least 85% by weight oi the polymer is acrylonitrile, in a solvent which does not react with or decompose the polymer and which may be substantially completely removed from the structures formed of such a solution.

It isanother object of this invention to produce a solution of polyacrylonitrile or-a copolymer or interpolymer of acrylonitrile in which at least 85% by weight of the polymer is acrylonitrile, in a solvent which does not react with or decompose the polymer, the solution being suitable for the formation of commercially useful, void free articles of polyacrylonitrile, for example yarns which are suitable as textile yarns and films which are suitable as wrapping tissue.

'It is another object of this invention to produce a solutionvof polyacrylonitrile, or a copolymer or interpolymer of acrylonitrile in which at least 85% by weight of the polymer is acrylonitrile, in a volatile organic solvent, which solution is stable over extended periods of time and and is eminently suited for use in the manufacture of shaped articles such as yarns, films, tubes, straws, artiiicial horsehair, bristles and ribbons, or when highly concentrated, for use in the manufacture of molded articles.

It is a still further object of this invention to produce shaped articles and structures of polyacrylonitrile, or copolymers or intel-polymers of acrylonitrile in which at least 85% by weight of the polymer is acrylonitrile.

It is still another object of this invention to produce a shaped article or structure of polyacrylonitrile or copolymers or interpolymers of acrylonitrile in which at least 85% by Weight of the polymer is acrylonitrile, for example a yarn, film, tube, bristle or the like which is tough, flexible, tenacious and free from voids.

Other objects of the invention will appear hereinafter.

Ihe objects of the invention may be accomplished in general by dissolving polyacrylonitrile, or a copolymer or interpolymer of acrylonitrile in which at least 85% by weight of the polymer is acrylonitrile, in an organic compound which is not a salt and which contains at least one dimethyl carbamyl group and at least one cyanomethylene group. If the solvent has a relatively low boiling point (less than about 250 C.), the solution of the acrylonitrile polymer` may then be formed into a .shaped structure, for example a yarn or film, and the solvent removed from the shaped structure to coagulate the same. When the solvent is relatively non-volatile and has a boiling point of about 300 C. or more, shaped articles may be made from the solution andl at least a portion of the solvent may be retained therein as a plasticizer for the articles.

It has been recognized in recent years that under certain conditions, an atom of hydrogen is attracted by rather strong forces to two atoms instead of only one, so that it may be considered to be acting as a bond between them. This is called the hydrogen bond.

The difficulty of dissolving polymers containing at least 85% by weight of acrylonitrile is due to ltion to dissolve an acrylonitrile polymer.

the presence within the molecules of strong hydrogen-bonding forces and in order to dissolve one of these polymers, it is necessary to 11nd a material which will undergo hydrogen bonding with the active hydrogen-bonding groups of the polymer molecules and thus weaken the strong hydrogen bond within the polymer molecules and cause the hydrogen-bonding forces to be shared between molecules of the polymer and the solvent. In this mannenit ispossible to form a molecular dispersion of the polymer within the solvent and thus form a solution.

However, the strength of the hydrogen-bonding capacity cannot be taken as the sole criterion as to whether or nota compound will func- It is also necessary that, in order to function as a cyano (-CENL thiocyano (-S-CEN) and sulfoxy (no EL lol...)

f rg.

groups, provided however that the cyano, thiocyano and sulfoxy groups require attachment (through their respective unsatisfied carbon and sulfur valences) to a carbon atom which is in turn attached to at least one hydrogen atom (alpha-hydrogen) in order to render them effective. The dimethyl carbamyl and the form'yl limido groups are effective in the absence of the alpha-hydrogen atom. (It is possible that they contain the equivalent of an alpha-hydrogen atom within their own structures.) lThus, the groups dimethyl carbamyl CH; o

formyl imido (HCON cyanomethylene CHCN)., thiocyanomethylene CHSCN) and sulfoxymethylene CHSO, CHSOz-,

CHSOO-, and CHSOzO-) shall hereinafter be referred to as solvogenic groups and compounds containing them are frequently capable of dissolving an acrylonitrile polymer containing at least by weight of acrylonitrile.

In the event that two or more groups requiring the presence of an alpha-hydrogen atom in order to render them solvogenic are attached to the Same carbon atom and compete with each other amarre merely'the nature of an inert substituent on the carbon atom.

It has furthermore been found that compounds containing the above-mentioned solvogenic groups will be solvents for the above-mentioned polymers only if the carbon content of the compound be within certain limits as given below. If the ratio of carbon to solvogenic groupings is maintained within the said limits, the compounds Will retain solvent properties of the polymer leven though the molecule be of considerable size and complexity. The solvent power of the compound for acrylonitrile polymers is increased if additional solvogenic groups are present in the molecular structure of the compound, the eect of these groups being additive.

It has now been found that dimethyl carbamyl cyanomethylene compounds which are fusible Without decomposition embraced by the following formula and preferably having a boiling point below 250 C. will dissolve polyacrylonitrile, and copolymers and interpolymers of acrylonitrile in which at least 85% by Weight of the polymer is acrylonitrile:

wherein m and q are integers equal to or greater than l.; n and p are integers of such value that n/m is equal to or less than 1.5 and p/q is equal to or less than 1.5.

These compounds are not salts but may be cyclic or acyclic in nature and may contain one or more ethylenic or acetylenic linkages. Valences other than those contained in the carbonto-carbon linkages and not shown as satised by the above formula must be satisfied by a substituent taken from the group consisting or hydrogen, halogen, oxygen, bivalent sulfur atoms and hydroxyl, thiol, cyano, thiocyano and sulfoxy radicals; the total number of halogen, oxygen and sulfur atoms and hydroxyl and thiol substituents not exceeding one-half the sum of m-l-q and the number of cyano, thiocyano and sulfoxy radicals not exceeding the sum of m-i-q. The respective tolerances of one-half m-i-q and m-l-q for the said two groups of substituents are independent of each other and members of said groups may be present in the molecule up to their group tolerances. substituent oxygen and sulfur atoms may appear in the compound as bivalent groups either as a side group (carbonyl or thiocarbonyl) or within the` chain (ether or thioether) as the case may be.

Representative compounds coming Within the scope of the above formula and suitable for use as solvents for the above-mentioned acrylonitrile polymers include:

NC-CHnC ON(CI Ia)2 N,Ndimethylcyanoacetamide NC-CHiCHnC ON(CHs):

Nc-onnrcomcm), N,N-dimethyl-alpha-bromo-alphacyenoacetamide C N (NC--CHaCHDzC C O N(CH|):

Gamma-(N,N-dimethylcarbamyl)-gammecyenopi melonitrile l N C-CEhCHC 0N(CHa)a H2O 0N(C Ha) a N,N,NN'tetramethylalphacyano-methyl-suocinamide C Ha C N C HaJJH-H-C oNmHm N,N-dimethyl-alpha-cyanoiso-valeramide C N CHsflJHC ON(CHu):

N,N-dimethyl-alpha-cyano-propiona mide C N CHaCHzCHaCHC ON(CBa)2 N ,N-dimethyl-alpha-cyano-valeramide y 0N CN c HaCHQCHfcHCC omonm i N, Ndimethyl-alpha,betadicyanocaproamide emcHCmCoNwHm N,N-dimethyl-beta-oyano-butyramide N C-C HzCHnCHsCHqC 0N(CHu) a N,N-dimethyldeltacyanoveleramide CHaCHCHaCHrC ON(CH)2 g N,N-dimethyl-gamma-cyano-valeramide C Ha NC-CHtlJC ON(CHa)| N ,N-alpha,alpha-tetramethyl-beta-cyanopropionamide l C Hs C N NC-CHzHCCONwHsh N,N-dimethyl-alpha-gamma-dicyanoisovaleramide C Hs NC-CHNJHCHC ON (CHs): N,Ndimethyl-gamma-cyanoisovaleramide NG-CHIC omemmn N,N,N'Ntetramethyl-cyanomalonamide above room temperature. Shaped structures and articles can be produced by extruding many of such solutions into an evaporative or coagulative medium. By forming the structures in an evaporative medium, the solvent must be evaporated therefrom and by forming the structures in a coagulative medium, the solvent should be removed by selective, solution in a non-solvent for the polymer. A

The solutions are prepared by `dissolving the polyacrylonitrile, or copolymer or interpolymer of acrylonitrile with one or a mixture of the above-mentioned solvents. Some of these solvents are solid at ordinary temperatures and dissolve or retain the polymer in clear solution only at elevated temperatures', for example at temperatures of 100 C. or higher, below which temperature the composition resembles a gel. In all cases when the polymer is dissolved in a solvent of the above class, the resulting composition while hot has the appearance of a true solution. When cooled to room temperature, the composition generally takes on the appearance of a gel, which gel may, on standing, undergo syneresis. Reheating of this gel or syneresed mass however causes it to again return to solution form.

In view `of the relatively high melting points of some of the solvents of this invention, they would have comparatively little use in the -production of a polyacrylonitrile spinning or casting solution. Such solvents are, however, excellent solvent plasticizers for polyacrylonitrile since they are soluble in a wide range of proportions with the said acrylonitrile polymers. The present invention therefore contemplates solid solu tions of acrylonitrile polymers containing at least 85% by weight of acrylonitrile as well as liquid solutions thereof. f

Shaped articles obtained from solvent solutions of pols/acrylonitrile in accordance with the invention and from which the solvent is subsequently removed are substantially free of foreign matter and voids and substantially undecomposed and chemically unchanged from the simple polymer prior to its solution.

The above-described organic solvent solutions of acrylonitrile polymer may be shaped in the form of filaments, yarns, films, tubes and like structures by apparatus and processes generally known in the art, the detailed operating conditions being suitably modied.

Suitable methods and apparatus for the production of shaped articles of the polymers of this invention will be readily apparent by reference to the following detailed description when taken in connection with the accompanying illustrations in which:

Figure 1 is a diagrammatic vertical sectional view showing a dry spinning cell suitable for use in accordance with the invention;

Figure 2 is a diagrammatic perspective view showing a lyarn drawing device for use in connection with the invention;

Figure 3 is a diagrammatic perspective view showing a wet spinning apparatus for use in the invention; and

Figure 4 is a diagrammatic side elevational view showing a suitable film casting apparatus for use in accordance with the invention. I

Referring to Figure 1 of the drawing, reference numeral I I designates a spinneret through whichv a plurality of filaments I5 are formed by extruding a lament-forming solution supplied to the spinneret by means of conduit I3. The spinning cell is jacketed with a material II., such as a re-` e i fractory in which is embedded an electrical heating coil I9. The spinning cell can thus be operated at any desired temperature. A plurality of conduits 2| are provided adjacent thebottomV of the device vfor passing evaporative medium through the cell so as to evaporate the solvent from the extruded filaments I5. The.evapora tive medium is removed from the cell through loutlet openings '23.A The yarn comprising the plurality of filaments I5 is passed from the bottom of the spinning cell around guide roller 25 and is wound on a bobbin 21.

Referring to Figure 2 of the drawing, the yarn l5 is removed from the bobbin package 2i and passed about draw roller 29 and separating roller 3I. From draw roller 29, the yarn is passed to a second draw roller 33 and separating roller 35.

The yarn is passed around the two sets of draw rollers including their separating rollers a sumcient number of turns to prevent slippage of the yarn. Draw roller 33 is rotated at a greater speed, for example three to ten times the speed of draw roller 29. In this manner, the yarn E5 is stretched between the two draw rollers. As the yarn passes between the two draw rollers, a heating medium is brought into contact with the yarn through blower nozzles 3i and 39. The yarn passing from the draw roller 33 is wound on bobbin 0I. The-drawing or stretching of the spun yarn as described is not claimed as part of the present invention, but is claimed in the copending application of Daniel T. Meloon, Serial No. 496,397, filed July 28, 1943.

Figure 3 of the drawing illustrates a wet spinning apparatus for the production of yarn. The acrylonitrile polymer solution is passed through conduit 5I and is extruded through spinneret 53 to form a multiiilament yarn Sli. The yarn 50 is passed about guide roller 5l which is positioned within the coagulating liquid in tank 55. The yarn is then passed about guide roller 5S and is wound on bobbin 0I.

The organic solvent solution of polyacrylonitrile may be cast in the form of a film as illustrated in Figure 4. In accordance with this apparatus, the polymer solution is passed from hopper l! on to the endless steel band 'i3 where it is smoothed by means of a doctor knife '85. The band, together with the film, is passed under a means Il for bringing a heated drying medium into contact with the film. The film 0I is pulled from the band 'I3 and collected on a mill roll 03.

The polyacrylonitrile for use with the invention is preferably prepared by the ammonium persulfate catalyzed polymerization of monomeric acrylonitrile dissolvedor emulsifieddn water. It can, however, be preparedby any other suitable type of polymerization reaction such as, for example, the emulsion type reaction disclosed by U. S. Patent No. 2,160,054 to Bauer et al. The polymer preferably possesses a molecular weight within the range of 15,000 to 250,000 or even higher, .as calculated from viscosity measurements by the Staudinger equation:

- 'N., Molecular Weight- Km0 wherein:

C=concentration of the solution expressed as the number of moles of the monomer (calculated) per liter of solution.

1I The molecular weight of the polymer obtained .is dependent on such factors as the concentra.-

tion of the monomer in the water, the amount and type of catalyst present, the temperature of the reaction, etc. For example, polyacrylcnitrile, having a molecular weight of approximately 60,000 can be prepared as follows: To 94 pounds of distilled water heated to 40 C. add 40 grams of ammonium persulfate-catalyst and 80 grams of sodium bisulilte activator. Then add 16 pounds of acrylonitrile slowly with stirring over a period of two hours.v The polyacrylonitrile having the above said molecular weight will precipitate fromthe solution. Increasing or decreasing the amount of the catalyst, while maintaining the other `conditions constant, decreases or increases the molecular'weight of the polymer. Acrylo- L nitrile copolymers and interpolymers containing Example I Fifteen parts of an acrylonitrile polymer prepared by the polymerization of monomeric acrylonitrile in accordance with the disclosure of U. S. Patent No. 2,160,054 to Bauer et al.` and possessing an average molecular weight of 120,000 as determined by the Staudinger equation from viscosity data were ground to an average particle size of 200 mesh and intimately mixed with 85 parts of similarly ground dimethyl cyano acetamide. The mixture was heated to 120 C. to form a clear, homogeneous dispersion or solution. When cooled to room temperature, it set to a clear, gel-like mass, which mass however again returned to solution form upon-heating to above 60 C. The solution heated to a temperature of 100 C. was extruded through a 10-hole spinneret (hole diameter of 0.003 inch) into a bath comprising glycerol heated to a temperature of 140 C. Y-The resulting multilament yarn of acrylonitrile polymer was washed with water and` dried.

Example II Forty (40) parts of the acrylonitrile polymer of Example I were mixed vwith 60 parts of gammamethyl-gamma-NN-dimethyl carbamyl pimelo- -nitrile and heated to a temperature of 175 C. to form a clear, homogeneous dispersionl or solution. I'he solution was cooled to 25 C. to form a clear, solid mass which was ground to a iine particle size f mesh). This powdery mass was molded at a temperature of 200 C. and a prese at least 85% by weight of acrylonitrile and like- 12 in the coating of wire and electrical parts where the high chemical and electrical resistance of the polymer is important.

For the purpose of definition, a solvent is a material which, when in the liquid state, is capable of forming solutions in which the polymer is present in a concentrationl by weight of 5% In most instances, the polymer is soluble in almost all proportions although the miscibility may take place at elevated temperatures in the case of certaincompounds.

As also shown, the solvents of the invention are useful not only in connection with polyacrylonitrile, but also with copolymers and interpolymers of acrylonitrile and with other poly- `merizable substances such as, for example, compounds containing one or more ethylenic linkages including vinyl and acrylic compounds as ,Y Well as olenic or diolefinic hydrocarbons such as isobutylene, butadiene, etc. They are eminently satisfactory'for use with those polymers that contain an appreciablevamount of acrylonitrile, for example, polymers, copolymers and interpolymers that contain at least by weight of acrylonitrile and that have generally been regarded by the art as being completely insoluble in all common organic solvents. Nor are these solvents limited to use with a polyacrylonitrile of any given molecular weight. They can be used with a polymer of' almost` any given molecular Weight and are especially satisfactory for use with those polymers having an average molecular weight within the range 15,000 to 250,000 as determined by viscosity data using the Staudinger equation and intended for. use in the manufacture of yarns or iilms.

The solution of acrylonitrile polymer dissolved in an organic solvent in accordance with thisinvention must be of such a concentration that its viscosity at the operating temperature is within a workable range. When it is to be employed in the spinning of yarn or the casting of lm, the solution should preferably have a viscosity within the range 25 to 750 poises. When the polymer has a molecular Weight of 250,000 or more, this requires that the maximum concentration of polymer in the spinning solution be of the o rder of 10%. Generally, it is preferred that the spinning solution contain at least 10% of the polymerv because of the diiculty of rapidly removing large amounts of solvent from the solution in the spinning operation. Moreover, it is economically undesirable to use such large amounts of solvent for the spinning of a given amount of polymer although it is true that the solvent can be completely recovered from the spinning operation and reused. For these reasons, itis preferred to employ a polymer having an` average molecular weight of lbetween 40,000 and 150,000 since such la polymer forms a solution of the desired viscosity in concentrations of the order of 15% to 25% andat a desirable spinning temperature of the order of to 150 C. OI course, it is within the scope of the invention to heat the solution to a higher temperature, even to above the normal boiling point of the solvent, for the actual spinning operation. Here again, the controlling factor with regard to the temperature of the spinning solution is the viscosity of the solution.

The evaporative medium employed in the-dry spinning of filaments and yarns or the dry casting of films in accordance with this invention may be any vapor inert to the filmor filamentforming solution such as air, nitrogen, steam, etc., or any suitable mixture thereof. The temperature of the evaporative medium is dependent on such factors as the dimensions of the spinning cell, the composition and rate of extrusion of the spinning solution and the rate of flow of the Aevaporative medium. It is only necessary that these several factors be so correlated that the yarn or other shaped article leaving the spinning cell be sufficiently freed of the solvent so that it is solidified and capable of being wound into package form or otherwise collected.

As indicated in Example I above, shaped articles of acrylonitrile polymer can also be formed by extruding the spinning solution into a suitable precipitating bath comprising a liquid that is miscible with the solvent butis a chemically inert non-solvent for the acrylonitrile polymer. As examples of such a liquid may be mentioned water, glycerin, organic solvents such as alcohol, ether, etc., or aqueous solutions of salts, alkalines i or acids. The copending application of William W. Watkins, Serial No. 496,376, filed July 28, 1943,

covers the use of glycerol and aqueous solutions of salts as baths, preferably at elevated temperatures, for the wet spinning of acrylonitrile polymer yarn, from solutions of the polymer, preferably with substantial tension and stretch being applied vduring spinning.

The article of acrylonitrile polymer thus obtained can advantageously be subjected to ya stretching operation of the type employed in the above examples. This stretching is preferably performed by passing the yarn between two positively driven rollers, the peripheral speeds of which are so adjusted that the article is stretched from two to ten times its original length, preferably approximately six times its original length. This stretching of the formed article may be performed at any suitable time. However, in the case of articles formed by the wet spinning or casting technique, it is preferably performed before the article has been completely dried. The orientation of the structure thus obtained improves the physical properties of the structure including its tenacity, its resilience, etc.

This stretching of the shaped article can also be accomplished by causing the article, while passing between stretching rollersto contact .a heated stationary pin or to pass through an inert medium such as air, water, glycerin, etc. heated to a high temperature.V Obviously, the article must not be exposed to this high temperature for a period suiciently long Ito decompose the polymer. In general however, the time of contact of the article with the heated medium is so short that temperatures up to 250 C. can be employed. Although it is generally preferred to heat the article to a temperature of at least 100 C. during the stretching operation, this is not'essentlal. Desirable results can be obtained by stretching the article without the application of heat, for

example by stretching at room temperature.

In addition to acting as solvents for polyacrylonitrile, or copolymers of acrylonitrile, the aliphatic or arylaliphatic nitrile compounds of this invention, when present in small amounts, can also be used as plasticizing agents for the polymer and the higher boiling compounds of the in- `vention are especially suited for such use. At the same time, it is, of course, to be understood that non-solvent softeners, such as glycerol, can also be incorporated in the solutions ofthe invention. these materials remaining in the subsequently formed articles to impart a softening effect. If it is desired to use such plasticizing or 'softening agents with -polyacrylonitri1e, they are preferably i4 added in the desired amount to an already formed solution of the polymer in a lower boiling solvent, for example to a solution of the polymer in dimethyl cyano acetamide.

This invention is primarily concerned with' the steps of dissolving polyacrylonitrile in a suitable solvent to form a stable solution adapted for use in the manufacture of shaped articles of polyacrylonitrile. vIt is characteristic of the invention that the solutions provided by it are stable; the solvents do not cause a decomposition or chemical alterationy of the dissolved acrylonitrile polymer. At the same time, it is also'characteristic that the solvents provided by the invention are also useful in th'e dissolving of mixtures of polyacrylonitrile and adjuvants such as dye modifiers, linear polyamides such as nylon, derivatives of cellulose including cellulose ethers and esters, polymers of vinyl compounds such as vinyl chloride, vinyl acetate, acrylic acid, etc., which adjuvants may be incorporated in the acrylonitrile polymer solution to modify the properties, both chemical and physical, of the resulting shaped articles.

This invention provides a class of solvents for polyacrylonitrile, and copolymers and interpolymers of acrylonitrile which were heretofore considered substantially insoluble. The solvents are capable of forming with the polymer clear solutions that are stable for extended periods of time and are admirably suited for use as lacquers or coating compositions or in the manufacture of shaped articles of the polymer, for example by extrusion into an evaporative or coagulative medium, or bythe use of a molding technique.

The invention also provides a class of materials that'is. eminently suited for use in plasticizing structures comprising the acrylonitrile polymers. The materials provided by this invention are apparently true solvents for the above-mentioned'acrylonitrile polymers. They do not tend to react with or decompose the polymer, the polymerio material obtained from the solution of this invention apparently being the same identical chemical composition as the initial polymer.

Yarns, films and similar articles of polyacrylonitrile prepared from the solutions of this invention can be stretched to yield oriented structures that possess a high tenacity. a desirable elongation and a high' elastic recovery that compares favorably with that of silk. The articles are not contaminated with undesirable salts and they are substantially free of void spaces.

Reference, throughout the specication and claims, to acrylonitrile polymers, polymers of acrylonitrile, and copolymers and inter-polymers of acrylonitrile containing at least by weight of acrylonitrile signifies polymers containing in their molecules at least 85% by weight of the acrylonitrile unit which is considered to be present in the polymer molecule as the group Hr-(IJlEI-CN that is, at least 85% by weight or the reaetant material converted into and forming the poli' is acrylonitrile.

Since it is obvious that m changes and modifications can be made in the above described details without departing from the nature and a spirit of the invention, it is to be understoodthat the invention is not to bev limited to the details of acrylonitrile containing in the polymer molecule at least 85% by weight of aorylonitrile dissolved in a dimethyl amide nitrile compound, said compound embraced within the formula:

valences of said compound other than those contained in carbon-to-carbon linkages and not shown as satisfied in the formula being satisiied by a substituent. taken from the group consisting of hydrogen, halogen, oxygen, bivalent sulfur, hydroxyl, thiol, cyano, thiocyano and sulfoxy; the total number of halogen, oxygen, sulfur, hydroxyl and thiol substituents not exceeding one half thev sum o 'm-i-q and the total number of cyano, thiocyano and sulfoxy radicals not exceeding the sum of m+q.

2. A new composition of matter as defined in claim 1 in which the polymer of acrylonitrile is polyacrylonitrile.

3. A new composition of matter as dened in claim 1 in which the polymer of acrylonitrile is non-reactive with said dimethyl amide nitrile compound.

4. A new composition of matter as dened in claim 1, in which said polymer is non-reactive with said dimethyl amide nitrile compound, but is soluble in all proportions therewith,

5. A new composition of matter as dened in claim 1, in which the polymer of acrylonitrile has a molecular weight of between 15,000 and 250,000.

6. A new composition of matter as dened in 'claim l, in which the polymer of acrylonitrile has a molecular weight of between 40,000 and 150,000. '7. A new composition of matter as defined in claim 1, in which the polymer solution has a viscosity between 25 and 750 poises.

8. lAs a new .composition of matter, a polymer of acrylonitrile containing in the polymer` molecule at least 85% by weight' of acrylonitrile dissolved Ain N,Ndimethylcyanoacetamide.

9. As a newv composition oi matter, a polymer of acrylonitrile containing in the polymer mole- -Certicate of Correction Patent No. 2,404,716.

numbered patent re airingl correction as niti'ile read polyacry onitmie; column 5, line 32; column l5,

for the indistinct subscript read p; column 7, lines 66 to 68, for that portion oi the i6, line 15, claim ll,

columny 13,` line 19, for alkalines read alkalies; and that the said should be read with these corrections therein that the same may conform of the case in the Patent Oiice.

16 cule at least 85% by weight of acrylonitrile dissolved in N,Ndimetliylbetacyano propionamide.

10. As a new composition of matter, a polymer of acrylonitrile containing in the polymer molecule at least 85% by Weight of acrylonitrile dissolved in beta-cyano-beta'(N,Ndimethylcarba myl) diethyl ether,

11. As a new composition of matter, a polymer of acrylonitrile containing in the polymer molecule at least 85% by weight of acrylonitrile and a dimethyl amide nitrile compound, said compound embraced within the formula: v

tol-t teal tained in carbon-to-carbon linkages and not shown as satised in the formula being satised by a substituent taken from the group consisting of hydrogen, halogen, oxygen, bivalent sulfur, hydroxyl, thiol, cyano, thiocyano and sulfoxy; the total number of halogen, oxygen, sulfur, hydroxyl and thiol substituentsnot exceeding one half the sum of m+q and the total number of cyano, thiocyano and sulfoxy radicals not exceeding the sum of m-i-q.

12. The composition of claim l in which the solution contains at least 10% of said polymer of acrylonitrile. I

13. The composition of claim 1 in which the polymer of acrylonitrile is polyacrylonitrile having a molecular weight of between 15,000 and which said polymer is polyacrylonitrile.

following 'VIRGIL L. HANSLEY.

July 23, 1946.

viRoiL L. HNSLEY It is hereby certified that errors'appear in the printed specification follows: Column. 2, line 9, for

of the above polyarcyloline 7, claim l, and column C after the third bracket, formula reading re'ad im Letters Patent to the record Signed and sealed this 5th day of November, A. D. 1946.

. LESLIE imma,

First Assistant Oommasoner of Patents. 

